接触素 5 和脂蛋白在阿尔茨海默病中的相互作用

M. Dauar, C. Picard, A. Labonté, John C S Breitner, P. Rosa-Neto, S. Villeneuve, Judes Poirier
{"title":"接触素 5 和脂蛋白在阿尔茨海默病中的相互作用","authors":"M. Dauar, C. Picard, A. Labonté, John C S Breitner, P. Rosa-Neto, S. Villeneuve, Judes Poirier","doi":"10.3233/JAD-231003","DOIUrl":null,"url":null,"abstract":"Background\nApolipoproteins and contactin 5 are proteins associated with Alzheimer's disease (AD) pathophysiology. Apolipoproteins act on transport and clearance of cholesterol and phospholipids during synaptic turnover and terminal proliferation. Contactin 5 is a neuronal membrane protein involved in key processes of neurodevelopment.\n\n\nObjective\nTo investigate the interactions between contactin 5 and apolipoproteins in AD, and the role of these proteins in response to neuronal damage.\n\n\nMethods\nApolipoproteins (measured by Luminex), contactin 5 (measured by Olink's proximity extension assay), and cholesterol (measured by liquid chromatography mass spectrometry) were assessed in the cerebrospinal fluid (CSF) and plasma of cognitively unimpaired participants (n = 93). Gene expression was measured using polymerase chain reaction in the frontal cortex of autopsied-confirmed AD (n = 57) and control subjects (n = 31) and in the hippocampi of mice following entorhinal cortex lesions.\n\n\nResults\nContactin 5 positively correlated with apolipoproteins B (p = 5.4×10-8), D (p = 1.86×10-4), E (p = 2.92×10-9), J (p = 2.65×10-9), and with cholesterol (p = 0.0096) in the CSF, and with cholesterol (p = 0.02), HDL (p = 0.0143), and LDL (p = 0.0121) in the plasma. Negative correlations were seen between CNTN5, APOB (p = 0.034) and APOE (p = 0.015) mRNA levels in the brains of control subjects. In the mouse model, apoe and apoj gene expression increased during the reinnervation phase (p <  0.05), while apob (p = 0.023) and apod (p = 0.006) increased in the deafferentation stage.\n\n\nConclusions\nExtensive interactions were observed between contactin 5 and apolipoproteins and cholesterol, possibly due to neuronal damage. The alterations in gene expression of apolipoproteins suggest a role in axonal, terminal, and synaptic remodeling in response to entorhinal cortex damage.","PeriodicalId":219895,"journal":{"name":"Journal of Alzheimer's disease : JAD","volume":"16 4","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Contactin 5 and Apolipoproteins Interplay in Alzheimer's Disease.\",\"authors\":\"M. Dauar, C. Picard, A. Labonté, John C S Breitner, P. Rosa-Neto, S. Villeneuve, Judes Poirier\",\"doi\":\"10.3233/JAD-231003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background\\nApolipoproteins and contactin 5 are proteins associated with Alzheimer's disease (AD) pathophysiology. Apolipoproteins act on transport and clearance of cholesterol and phospholipids during synaptic turnover and terminal proliferation. Contactin 5 is a neuronal membrane protein involved in key processes of neurodevelopment.\\n\\n\\nObjective\\nTo investigate the interactions between contactin 5 and apolipoproteins in AD, and the role of these proteins in response to neuronal damage.\\n\\n\\nMethods\\nApolipoproteins (measured by Luminex), contactin 5 (measured by Olink's proximity extension assay), and cholesterol (measured by liquid chromatography mass spectrometry) were assessed in the cerebrospinal fluid (CSF) and plasma of cognitively unimpaired participants (n = 93). Gene expression was measured using polymerase chain reaction in the frontal cortex of autopsied-confirmed AD (n = 57) and control subjects (n = 31) and in the hippocampi of mice following entorhinal cortex lesions.\\n\\n\\nResults\\nContactin 5 positively correlated with apolipoproteins B (p = 5.4×10-8), D (p = 1.86×10-4), E (p = 2.92×10-9), J (p = 2.65×10-9), and with cholesterol (p = 0.0096) in the CSF, and with cholesterol (p = 0.02), HDL (p = 0.0143), and LDL (p = 0.0121) in the plasma. Negative correlations were seen between CNTN5, APOB (p = 0.034) and APOE (p = 0.015) mRNA levels in the brains of control subjects. In the mouse model, apoe and apoj gene expression increased during the reinnervation phase (p <  0.05), while apob (p = 0.023) and apod (p = 0.006) increased in the deafferentation stage.\\n\\n\\nConclusions\\nExtensive interactions were observed between contactin 5 and apolipoproteins and cholesterol, possibly due to neuronal damage. The alterations in gene expression of apolipoproteins suggest a role in axonal, terminal, and synaptic remodeling in response to entorhinal cortex damage.\",\"PeriodicalId\":219895,\"journal\":{\"name\":\"Journal of Alzheimer's disease : JAD\",\"volume\":\"16 4\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-04-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Alzheimer's disease : JAD\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3233/JAD-231003\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Alzheimer's disease : JAD","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3233/JAD-231003","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

背景载脂蛋白和接触素 5 是与阿尔茨海默病(AD)病理生理学相关的蛋白质。载脂蛋白在突触转换和末端增殖过程中起着运输和清除胆固醇和磷脂的作用。目的 研究接触素 5 和载脂蛋白在 AD 中的相互作用,以及这些蛋白在神经元损伤中的作用。方法对认知功能未受损的参与者(93 人)的脑脊液(CSF)和血浆中的脂蛋白(用 Luminex 测定)、接触素 5(用 Olink 的接近延伸测定法测定)和胆固醇(用液相色谱质谱法测定)进行评估。使用聚合酶链反应测量了经尸检证实的 AD 患者(57 人)和对照组患者(31 人)的额叶皮层以及内叶皮层病变后小鼠海马中的基因表达。4×10-8)、D(p = 1.86×10-4)、E(p = 2.92×10-9)、J(p = 2.65×10-9)以及脑脊液中的胆固醇(p = 0.0096)和血浆中的胆固醇(p = 0.02)、高密度脂蛋白(p = 0.0143)和低密度脂蛋白(p = 0.0121)呈正相关。对照组大脑中 CNTN5、APOB(p = 0.034)和 APOE(p = 0.015)mRNA 水平呈负相关。在小鼠模型中,apoe 和 apoj 基因表达在神经再支配阶段增加(p < 0.05),而 apob(p = 0.023)和 apod(p = 0.006)在去神经支配阶段增加。脂蛋白基因表达的改变表明,脂蛋白在轴突、末梢和突触重塑中扮演着重要角色,以应对内叶皮层损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Contactin 5 and Apolipoproteins Interplay in Alzheimer's Disease.
Background Apolipoproteins and contactin 5 are proteins associated with Alzheimer's disease (AD) pathophysiology. Apolipoproteins act on transport and clearance of cholesterol and phospholipids during synaptic turnover and terminal proliferation. Contactin 5 is a neuronal membrane protein involved in key processes of neurodevelopment. Objective To investigate the interactions between contactin 5 and apolipoproteins in AD, and the role of these proteins in response to neuronal damage. Methods Apolipoproteins (measured by Luminex), contactin 5 (measured by Olink's proximity extension assay), and cholesterol (measured by liquid chromatography mass spectrometry) were assessed in the cerebrospinal fluid (CSF) and plasma of cognitively unimpaired participants (n = 93). Gene expression was measured using polymerase chain reaction in the frontal cortex of autopsied-confirmed AD (n = 57) and control subjects (n = 31) and in the hippocampi of mice following entorhinal cortex lesions. Results Contactin 5 positively correlated with apolipoproteins B (p = 5.4×10-8), D (p = 1.86×10-4), E (p = 2.92×10-9), J (p = 2.65×10-9), and with cholesterol (p = 0.0096) in the CSF, and with cholesterol (p = 0.02), HDL (p = 0.0143), and LDL (p = 0.0121) in the plasma. Negative correlations were seen between CNTN5, APOB (p = 0.034) and APOE (p = 0.015) mRNA levels in the brains of control subjects. In the mouse model, apoe and apoj gene expression increased during the reinnervation phase (p <  0.05), while apob (p = 0.023) and apod (p = 0.006) increased in the deafferentation stage. Conclusions Extensive interactions were observed between contactin 5 and apolipoproteins and cholesterol, possibly due to neuronal damage. The alterations in gene expression of apolipoproteins suggest a role in axonal, terminal, and synaptic remodeling in response to entorhinal cortex damage.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信